Genes involved in osmoregulation during turgor-driven cell expansion of developing cotton fibers are differentially regulated

Plant Physiol. 1998 Apr;116(4):1539-49. doi: 10.1104/pp.116.4.1539.

Abstract

Cotton (Gossypium hirsutum L.) fibers are single-celled trichomes that synchronously undergo a phase of rapid cell expansion, then a phase including secondary cell wall deposition, and finally maturation. To determine if there is coordinated regulation of gene expression during fiber expansion, we analyzed the expression of components involved in turgor regulation and a cytoskeletal protein by measuring levels of mRNA and protein accumulation and enzyme activity. Fragments of the genes for the plasma membrane proton-translocating ATPase, vacuole-ATPase, proton-translocating pyrophosphatase (PPase), phosphoenolpyruvate carboxylase, major intrinsic protein, and alpha-tubulin were amplified by polymerase chain reaction and used as probes in ribonuclease protection assays of RNA from a fiber developmental series, revealing two discrete patterns of mRNA accumulation. Transcripts of all but the PPase accumulated to highest levels during the period of peak expansion (+12-15 d postanthesis [dpa]), then declined with the onset of secondary cell wall synthesis. The PPase was constitutively expressed through fiber development. Activity of the two proton-translocating-ATPases peaked at +15 dpa, whereas PPase activity peaked at +20 dpa, suggesting that all are involved in the process of cell expansion but with varying roles. Patterns of protein accumulation and enzyme activity for some of the proteins examined suggest posttranslational regulation through fiber development.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Blotting, Western
  • Cloning, Molecular
  • Gene Expression Regulation, Enzymologic*
  • Gene Expression Regulation, Plant*
  • Gossypium / enzymology
  • Gossypium / genetics
  • Gossypium / growth & development*
  • Osmosis
  • Polymerase Chain Reaction
  • Protein Processing, Post-Translational
  • Proton-Translocating ATPases / genetics
  • Proton-Translocating ATPases / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Vacuolar Proton-Translocating ATPases*

Substances

  • RNA, Messenger
  • Vacuolar Proton-Translocating ATPases
  • Proton-Translocating ATPases